| Tag | Content |
|---|
EnhancerAtlas ID | HS187-20104 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr5:140971620-140972380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr5:140971911-140971927 | TATTGTTTACTTAGTT | - | 6.46 | | Foxa2 | MA0047.2 | chr5:140971914-140971926 | TGTTTACTTAGT | + | 6.44 | | IRF1 | MA0050.2 | chr5:140971652-140971673 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_22802 | chr5:140971733-140973364 | CD8_primiary | | SE_51634 | chr5:140971506-140973303 | Skeletal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I141592 | chr5 | 140971681 | 140971870 |
|
Enhancer Sequence | TCTGGGTGAC AGAGCGAGAC TCTGTATCAA AAAAAAAAAA AAAGAAAGAA AGAAAATTTA 60
AAAAAAATTA CCCATGTTTT AGTGTTCAAT TTGGGGAAGG ACAGCAAACA TGATCCACGA 120
GGGAAAAAAA GCTGCATTTC CTGAGCTAGT CCAACAGAGG GCAGCAACAA CCAGCAAAGT 180
GAATCACAGC CCAGTCAGTA CAAGCAAAAC GGTTTTAGAA TCCAATACAA CACTCAAACA 240
GCAAGCTCAA TTATTAAAAT AGAAACCTGC TGCTACAGTA TATTCAGAGT GTATTGTTTA 300
CTTAGTTAAT ACTATGTGTG TTCTTACAGA TTCTATGTTG GCAAACAGCT TTGTTCAGTA 360
GTCATTTTTT AATTGTATCA TTAGTTGTGT GTATTCTCTG AAATATAGAA TAAGTTCCTA 420
GATCATGACA AGTTAACAAC AACAACAACA ACAACAACAA CAACAACAAA AACACAGGAG 480
TCCAGGGAGA TAAATGCTAC TGGAGCTTTA TTTATGTATT AGGTCTCAGA TATCCAAGAT 540
TCTTAAAATT AAGTCTCTAA TCATCCTACC TACATCTAAA TGCATCCACT TTCATCATTC 600
TCCTTGTTTG CTGTCAATTC TCTTCTGGTC CCAAACCAAA CCCTTACTGT CCTAGGCTGG 660
CTGTGGTAAA TATCTCACTT CCTGGCCCTT CTATTGAGTC CTCCACTAAA CATTAGCACT 720
TATACCTTTA ACTACAAATA TAGATACTGA AGGAAGCATA 760
|
